| Literature DB >> 20683999 |
Adeline Jacquinet1, Marion Gérard, Michael T Gabbett, Léon Rausin, Jean-Paul Misson, Björn Menten, Geert Mortier, Lionel Van Maldergem, Alain Verloes, François-Guillaume Debray.
Abstract
Temple-Baraitser syndrome, previously described in two unrelated patients, is the association of severe mental retardation and abnormal thumbs and great toes. We report two additional unrelated patients with Temple-Baraitser syndrome, review clinical and radiological features of previously reported cases and discuss mode of inheritance. Patients share a consistent pattern of anomalies: hypo or aplasia of the thumb and great toe nails and broadening and/or elongation of the thumbs and halluces, which have a tubular aspect. All patients were born to unrelated parents and occurred as a single occurrence in multiple sibships, suggesting sporadic inheritance from a de novo mutation mechanism. Comparative genomic hybridization in Patients 1, 2 and 3 did not reveal any copy number variations. We confirm that Temple-Baraitser syndrome represents a distinct syndrome, probably unrecognized, possibly caused by a de novo mutation in a not yet identified gene.Entities:
Mesh:
Year: 2010 PMID: 20683999 DOI: 10.1002/ajmg.a.33574
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802